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CoMPARA : Collaborative Modeling Project for Androgen Receptor Activity

Authors :
Mansouri, Kamel
Kleinstreuer, Nicole
Abdelaziz, Ahmed M.
Alberga, Domenico
Alves, Vinicius M.
Andersson, Patrik L.
Andrade, Carolina H.
Bai, Fang
Balabin, Ilya
Ballabio, Davide
Benfenati, Emilio
Bhhatarai, Barun
Boyer, Scott
Chen, Jingwen
Consonni, Viviana
Farag, Sherif
Fourches, Denis
García-Sosa, Alfonso T.
Gramatica, Paola
Grisoni, Francesca
Grulke, Chris M.
Hong, Huixiao
Horvath, Dragos
Hu, Xin
Huang, Ruili
Jeliazkova, Nina
Li, Jiazhong
Li, Xuehua
Liu, Huanxiang
Manganelli, Serena
Mangiatordi, Giuseppe F.
Maran, Uko
Marcou, Gilles
Martin, Todd
Muratov, Eugene
Nguyen, Dac-Trung
Nicolotti, Orazio
Nikolov, Nikolai G.
Norinder, Ulf
Papa, Ester
Petitjean, Michel
Pür, Geven
Pogodin, Pavel
Poroikov, Vladimir
Qiao, Xianliang
Richard, Ann M.
Roncaglioni, Alessandra
Ruiz, Patricia
Rupakheti, Chetan
Sakkiah, Sugunadevi
Sangion, Alessandro
Schramm, Karl-Werner
Selvaraj, Chandrabose
Shah, Imran
Sild, Sulev
Sun, Lixia
Taboureau, Olivier
Tang, Yun
Tetko, Igor V.
Todeschini, Roberto
Tong, Weida
Trisciuzzi, Daniela
Tropsha, Alexander
Van Den Driessche, George
Varnek, Alexandre
Wang, Zhongyu
Wedebye, Eva B.
Williams, Antony J.
Xie, Hongbin
Zakharov, Alexey V.
Zheng, Ziye
Judson, Richard S.
Mansouri, Kamel
Kleinstreuer, Nicole
Abdelaziz, Ahmed M.
Alberga, Domenico
Alves, Vinicius M.
Andersson, Patrik L.
Andrade, Carolina H.
Bai, Fang
Balabin, Ilya
Ballabio, Davide
Benfenati, Emilio
Bhhatarai, Barun
Boyer, Scott
Chen, Jingwen
Consonni, Viviana
Farag, Sherif
Fourches, Denis
García-Sosa, Alfonso T.
Gramatica, Paola
Grisoni, Francesca
Grulke, Chris M.
Hong, Huixiao
Horvath, Dragos
Hu, Xin
Huang, Ruili
Jeliazkova, Nina
Li, Jiazhong
Li, Xuehua
Liu, Huanxiang
Manganelli, Serena
Mangiatordi, Giuseppe F.
Maran, Uko
Marcou, Gilles
Martin, Todd
Muratov, Eugene
Nguyen, Dac-Trung
Nicolotti, Orazio
Nikolov, Nikolai G.
Norinder, Ulf
Papa, Ester
Petitjean, Michel
Pür, Geven
Pogodin, Pavel
Poroikov, Vladimir
Qiao, Xianliang
Richard, Ann M.
Roncaglioni, Alessandra
Ruiz, Patricia
Rupakheti, Chetan
Sakkiah, Sugunadevi
Sangion, Alessandro
Schramm, Karl-Werner
Selvaraj, Chandrabose
Shah, Imran
Sild, Sulev
Sun, Lixia
Taboureau, Olivier
Tang, Yun
Tetko, Igor V.
Todeschini, Roberto
Tong, Weida
Trisciuzzi, Daniela
Tropsha, Alexander
Van Den Driessche, George
Varnek, Alexandre
Wang, Zhongyu
Wedebye, Eva B.
Williams, Antony J.
Xie, Hongbin
Zakharov, Alexey V.
Zheng, Ziye
Judson, Richard S.
Publication Year :
2020

Abstract

BACKGROUND: Endocrine disrupting chemicals (EDCs) are xenobiotics that mimic the interaction of natural hormones and alter synthesis, transport, or metabolic pathways. The prospect of EDCs causing adverse health effects in humans and wildlife has led to the development of scientific and regulatory approaches for evaluating bioactivity. This need is being addressed using high-throughput screening (HTS) in vitro approaches and computational modeling. OBJECTIVES: In support of the Endocrine Disruptor Screening Program, the U.S. Environmental Protection Agency (EPA) led two worldwide consortiums to virtually screen chemicals for their potential estrogenic and androgenic activities. Here, we describe the Collaborative Modeling Project for Androgen Receptor Activity (CoMPARA) efforts, which follows the steps of the Collaborative Estrogen Receptor Activity Prediction Project (CERAPP). METHODS: The CoMPARA list of screened chemicals built on CERAPP's list of 32,464 chemicals to include additional chemicals of interest, as well as simulated ToxCast (TM) metabolites, totaling 55,450 chemical structures. Computational toxicology scientists from 25 international groups contributed 91 predictive models for binding, agonist, and antagonist activity predictions. Models were underpinned by a common training set of 1,746 chemicals compiled from a combined data set of 11 ToxCast (TM)/Tox21 HTS in vitro assays. RESULTS: The resulting models were evaluated using curated literature data extracted from different sources. To overcome the limitations of single-model approaches, CoMPARA predictions were combined into consensus models that provided averaged predictive accuracy of approximately 80% for the evaluation set. DISCUSSION: The strengths and limitations of the consensus predictions were discussed with example chemicals; then, the models were implemented into the free and open-source OPERA application to enable screening of new chemicals with a defined applicability domain and accura

Details

Database :
OAIster
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1234705681
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1289.EHP5580